Canonical Allele Identifier: PA2828788633
Gene: SMAD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2381239
ClinVar RCV Id: RCV002679482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365550.1:p.Val95Leu
CA248181295
NM_001378621.1:c.283G>T
CA387852645
NM_001378621.1:c.283G>C